Clinical Trials Logo

Diabetic Gastroparesis clinical trials

View clinical trials related to Diabetic Gastroparesis.

Filter by:

NCT ID: NCT01696747 Completed - Gastroparesis Clinical Trials

Gastroparesis Registry 2

GpR2
Start date: July 2012
Phase:
Study type: Observational

To expand a registry of patients for the study of the epidemiology, etiology, and degree of morbidity associated with gastroparesis.

NCT ID: NCT01664637 Terminated - Clinical trials for Diabetic Gastroparesis

Diabetic Gastroparesis Efficacy/Safety Study of TZP-102

DIGEST
Start date: August 2012
Phase: Phase 2
Study type: Interventional

The purpose of this study is to test the safety and effectiveness of 10 mg TZP-102 given prior to meals three times a day compared to placebo (capsule that looks like active study drug but contains no active drug), administered for 12 weeks, in diabetic subjects with symptoms associated with gastroparesis.

NCT ID: NCT01607684 Completed - Diabetes Mellitus Clinical Trials

Pilot Study to Evaluate Magnetic Marker Imaging on Diabetic Polyneuropathy and Gastroparesis

Start date: January 2012
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether Magnetic Marker Monitoring is an appropriate opportunity to diagnose and to quantify a suspicious gastroparesis in subjects with diabetic polyneuropathy.

NCT ID: NCT01557296 Completed - Clinical trials for Diabetic Gastroparesis

Evaluation of Diagnostic Methods and Dietary Treatment of Diabetic Gastroparesis

Start date: September 2007
Phase: Phase 2
Study type: Interventional

The objective of the study is in subjects with Insulin Treated Diabetes Mellitus type 1 or 2 and gastroparesis: - validate radiopaque markers with fluoroscopy with gastric scintigraphy method - study the difference of metabolic control including the frequents of hypoglycaemia, gastrointestinal symptoms, quality of life and nutrition state during dietary treatment of food of small particle size compared with food of large particle size - validate the radiopaque markers method and measurement of the blood glucose and gastrointestinal symptoms after a test meal, against the gastric scintigraphy - determine if the function of gastric emptying can be improved after intervention

NCT ID: NCT01469286 Completed - Clinical trials for Diabetic Gastroparesis

Transcutaneous Electroacupuncture for Gastroparesis

TEA
Start date: March 2010
Phase: Phase 1
Study type: Interventional

Gastroparesis is a common disease defined as delayed emptying of the stomach. It is present in at least 20% of about 150 million patients with diabetes worldwide and in more than 20% of patients with functional dyspepsia that affects about 10%-25% of the general population. Gastroparesis is a refractory disease with a lack of therapeutic options. Common symptoms of gastroparesis include nausea, vomiting, early satiety and abdominal bloating. Electroacupuncture (EA) is a combined procedure with acupuncture and electrical current stimulation instead of manual manipulations of the needles. Recent studies in our lab with EA or transcutaneous EA (TEA) have suggested a therapeutic role of EA or TEA for gastric motility disorders. Improvement has been observed with EA or TEA in gastric emptying as well as dyspeptic symptoms. In this project, a micro-stimulator is designed and developed for the TEA therapy. The micro-stimulator is small enough so that it can be attached to the skin next to the stimulation electrodes and therefore the patient can resume normal daily activity while being treated by TEA. This is not only attractive but also more effective since TEA can be performed more often and for longer durations. This exploratory project is designed to study the feasibility, efficacy and certain mechanisms of the proposed method of "wireless" TEA in patients with gastroparesis. Firstly the feasibility of the chronic use the proposed micro-stimulator will be studied. Secondly, the efficacy of the TEA in improving delayed gastric emptying and symptoms of gastroparesis will be investigated in a double-blinded crossover design in patients with diabetic or idiopathic gastroparesis. Thirdly, possible mechanisms involving pathogeneses of gastroparesis with TEA will be investigated.

NCT ID: NCT01326117 Withdrawn - Nausea Clinical Trials

Daily Tadalafil and Gastric Emptying Time in Diabetic Gastroparesis

Start date: April 2011
Phase: Phase 4
Study type: Interventional

The investigators hypothesize that in adult patients with diabetic gastroparesis with Type 1 diabetes (HbA1c ≤ 10.5%), daily tadalafil use will significantly improve gastric emptying compared to baseline as measured by gastric emptying time.

NCT ID: NCT01126034 Completed - Clinical trials for Gastroesophageal Reflux Disease

Improving Metoclopramide Prescribing Practices at Penn Through a Physician-targeted Intervention

Start date: March 2007
Phase: N/A
Study type: Interventional

The investigators hypothesized that: 1) an intervention targeted at the prescribing physician would increase the rate of a metoclopramide discontinuation among patients prescribed the medication for questionable or unclear indications; and 2) the discontinuation would be durable.

NCT ID: NCT01030341 Completed - Clinical trials for Diabetic Gastroparesis

Continuous Glucose Monitoring and Insulin Pump Therapy in Diabetic Gastroparesis

GLUMIT-DG
Start date: May 2011
Phase: N/A
Study type: Interventional

A pilot study to assess the safety, feasibility, and potential (uncontrolled) efficacy of continuous glucose monitoring (CGMS) in conjunction with an insulin pump to improve glycemic control for treatment of type 1 and type 2 diabetic patients with gastroparesis

NCT ID: NCT00944593 Withdrawn - Clinical trials for Diabetic Gastroparesis

Gastric vs Jejunal Feeding in Diabetic Gastroparesis

Start date: n/a
Phase: Phase 4
Study type: Interventional

Diabetic 'Gastroparesis' or 'Gastroenteropathy' is a condition in which patients suffer episodes of nausea, vomiting, abdominal bloating and pain after eating. These symptoms occur in the absence of any structural abnormality of the stomach, rather abnormal gastric function underlies the condition. Up to one in five patients with type I diabetes experience symptoms consistent with this diagnosis. The effects on diabetic control, physical health and emotional quality of life are severe. Patients do not respond reliably to general supportive management or conventional medications. Surgical options have disappointing results. The need for more effective treatment is acknowledged universally. Feeding into the small bowel beyond the stomach (jejunal feeding) is established management in diabetic patients with gastroenteropathy that are malnourished due to poor oral intake. The benefits have been assumed secondary to improved nutrition and diabetic control; however this assertion has never been studied. Recently we observed that patients with severe gastroenteropathy recovered promptly and could eat normally during and for a few hours after jejunal feeding. These observations suggest that jejunal feeding has 'quasi-pharmacological' effects in patients with gastroenteropathy. One attractive explanation for these observations is that gastroenteropathy represents a failure of oral intake to 'switch' the stomach from the fasted to the fed state. According to this hypothesis, jejunal feeding 'restores' the normal fed state by bypassing the dysfunctional stomach. This project will assess the effects of feeding on gastrointestinal (GI) sensory and motor function in diabetic gastroenteropathy. Healthy volunteers and diabetic controls without symptoms will also be investigated. Studies will assess: 1. Effects on GI symptoms and function to gastric distension in fasted and fed states 2. Effects on GI symptoms and function to oral vs. nasogastric delivery of a test meal 3. A trial of gastric feeding with and without prior jejunal feeding on GI symptoms and function Non-invasive magnetic resonance imaging (MRI) techniques will be applied to assess complex gastric response to feeding. In addition the effects of feeding on symptoms and gastric function will be related to alterations in GI hormones and autonomic nervous activity (eg cardiovagal tone) to assess how the integrated response of the GI tract to feeding fails in patients with diabetic gastroenteropathy. The primary aim of this project is to assess the effectiveness of jejunal feeding in the management of diabetic gastroenteropathy. However, by defining the processes that 'switch' gastric function between the fasted and the fed states and control gastric emptying, we hope also to identify candidate targets for more effective pharmacologic treatment of this severe disease. - Trial with medical device

NCT ID: NCT00874133 Terminated - Clinical trials for Diabetic Gastroparesis

The Effect of Acupuncture on Symptoms, Gastric Emptying Rate and Glucose Control in Patients With Diabetic Gastroparesis

Start date: March 2009
Phase: N/A
Study type: Interventional

Diabetes affects 5.8% of the adult population in Israel (1). Gastroparesis is a syndrome characterized by delayed gastric emptying in the absence of mechanical obstruction of the stomach.Treatment with acupuncture has been described as effective in improvement of symptoms in patients with gastroparesis in a number of patient series. However, this treatment approach has not been tested by means of a controlled randomized clinical study, and neither has the connection between improvement of symptoms and the anatomical-physiological effect of the treatment, if ever, assessed.This study will test the efficacy of motilium (20 mg thrice daily) as compared to acupuncture treatment on the following subjective and objective parameters of 30 patients with diabetic gastroparesis and impaired glucose control: 1. To compare the degree of GCSI scores improvement before and after treatment with motilium or acupuncture using a validated questionnaire. 2. To determine the effect of treatment with motilium or acupuncture on gastric emptying rate. 3. To determine the effect of treatment with motilium or acupuncture on glycemic control. 4. To compare the quality of life before and after treatment with motilium or acupuncture using the Short Form-36 (SF-36).